Age‐dependent cerebrospinal fluid‐tissue water exchange detected by magnetization transfer indirect spin labeling MRI

Author(s):  
Anna M. Li ◽  
Lin Chen ◽  
Hongshuai Liu ◽  
Yuguo Li ◽  
Wenzhen Duan ◽  
...  
2008 ◽  
Vol 54 (9) ◽  
pp. 1443-1450 ◽  
Author(s):  
Sabine A Fuchs ◽  
Monique G M de Sain-van der Velden ◽  
Martina M J de Barse ◽  
Martin W Roeleveld ◽  
Margriet Hendriks ◽  
...  

Abstract Background: The recent discovery and specific functions of d-amino acids in humans are bound to lead to the revelation of d-amino acid abnormalities in human disorders. Therefore, high-throughput analysis techniques are warranted to determine d-amino acids in biological fluids in a routine laboratory setting. Methods: We developed 2 chromatographic techniques, a nonchiral derivatization with chiral (chirasil-l-val column) separation in a GC-MS system and a chiral derivatization with Marfey’s reagent and LC- MS analysis. We validated the techniques for d-serine, l-serine, and glycine determination in cerebrospinal fluid (CSF), evaluated several confounders, and determined age-dependent human concentration ranges. Results: Quantification limits for d-serine, l-serine, and glycine in cerebrospinal fluid were 0.14, 0.44, and 0.14 μmol/L, respectively, for GC-MS and 0.20, 0.41, and 0.14 μmol/L for LC-MS. Within-run imprecision was <3% for both methods, and between-run imprecision was <13%. Comparison of both techniques with Deming regression yielded coefficients of 0.90 (d-serine), 0.92 (l-serine), and 0.96 (glycine). Sample collection, handling, and transport is uncomplicated—there is no rostrocaudal CSF gradient, no effect of storage at 4 °C for 1 week before storage at −80 °C, and no effect of up to 3 freeze/thaw cycles. Conversely, contamination with erythrocytes increased d-serine, l-serine, and glycine concentrations. CSF concentrations for 145 apparently healthy controls demonstrated markedly and specifically increased (5 to 9 times) d-serine concentrations during early central nervous system development. Conclusions: These 2 clinically applicable analysis techniques will help to unravel pathophysiologic, diagnostic, and therapeutic issues for disorders associated with central nervous system abnormalities, NMDA-receptor dysfunction, and other pathology associated with d-amino acids.


2006 ◽  
Vol 250 (1-2) ◽  
pp. 50-57 ◽  
Author(s):  
Sandra Ebert ◽  
David J. Phillips ◽  
Peter Jenzewski ◽  
Roland Nau ◽  
Anne E. O'Connor ◽  
...  

2001 ◽  
Vol 21 (4) ◽  
pp. 440-455 ◽  
Author(s):  
Jinyuan Zhou ◽  
David A. Wilson ◽  
John A. Ulatowski ◽  
Richard J. Traystman ◽  
Peter C. M. van Zijl

The original well-mixed tissue model for the arterial spin tagging techniques is extended to a two-compartment model of restricted water exchange between microvascular (blood) and extravascular (tissue) space in the parenchyma. The microvascular compartment consists of arterioles, capillaries, and venules, with the blood/tissue water exchange taking place in the capillaries. It is shown that, in the case of limited water exchange, the individual FAIR (Flow-sensitive Alternating Inversion Recovery) signal intensities of the two compartments are comparable in magnitude, but are not overlapped in time. It is shown that when the limited water exchange is assumed to be fast, flows quantified from the signal-intensity difference are underestimated, an effect that becomes more significant for larger flows and higher magnetic field strengths. Experimental results on cat brain at 4.7 T comparing flow data from the FAIR signal-intensity difference with those from microspheres over a cerebral blood flow range from 15 to 150 mL 100 g−1 min−1 confirm these theoretic predictions. FAIR flow values with correction for restricted exchange, however, correlate well with the radioactive microsphere flow values. The limitations of the approach in terms of choice of the intercompartmental exchange rates are discussed.


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